Chlorobium luteolum DSM 273 was formerly known as Pelodictyon luteolum DSM 273.

The green sulfur bacteria (GSB; Phylum Chlorobi ) are commonly found in illuminated, stratified, and anoxic aquatic environments, sediments, and other sulfide-rich environments including hot springs (1, 2). Because of unique adaptations of their light-harvesting antennae, these bacteria are capable of growth at light intensities under which no other phototrophs can survive (3). In some aquatic environments, these organisms can account for up to 83% of the total annual productivity, and thus it is clear that these organisms can be the primary contributors of fixed carbon in certain ecological niches.The known GSB are metabolic specialists: all strains are strictly anaerobic and obligately photoautotrophic in growth mode, and none is capable of dark respiratory or strictly fermentative metabolism. Most of these bacteria use electrons derived from reduced sulfur compounds in combination with light energy to reduce carbon and nitrogen (4). Many GSB strains can also utilize hydrogen as an electron donor for photoautotrophic growth. Thus, in anoxic environments, Chlorobi are very important compontents of the carbon, nitrogen, and sulfur cycles. Carbon fixation in the GSB occurs by the reverse TCA cycle reactions. The photosynthetic apparatus includes homodimeric Type I reaction centers that are distantly related to Photosystem I reaction centers of higher plants and cyanobacteria. The light harvesting antenna, chlorosomes, are ovoid bodies surrounded by a lipid monolayer and filled with more than 200,000 BChl c/d/e molecules and ~2500 BChl a molecules associated with the protein CsmA (5). Because a GSB cell can contain as many as 250 chlorosomes, a GSB cell may contain more than 50 million BChl molecules! It is these enormous antennae that allow the cells to perform photosynthesis at vanishingly low light conditions (4). Although GSB share some biochemical and metabolic properties with other phototrophs, 16S rRNA analyses indicate that these bacteria are only very distantly related to other phototrophs (cyanobacteria, purple bacteria (proteobacteria), heliobacteria, and filamentous anoxygenic phototrophs (green non-sulfur bacteria or Chloroflexaceae ). However, the Chlorobi seem to share a common ancestor with the Bacteroidetes (2).

Chlorobium luteolum strain DSMZ 273 T (formerly Pelodictyon luteolum strain DSMZ 273 T (6)) is non-motile, and forms short stumpy, rod-shaped cells (width: 0.6 to 0.9 µm; length 1.2 to 2.0 µm). Depending on culture conditions, the cells can form slime and become united into hollow, spherical or irregular, rounded colonies with the cells in a single layer. In contrast to the majority of GSB, Chl. luteolum forms gas vesicles. Due to its conspicuous morphology, Schmidle (7) had already described this bacterium (as an alga) in 1901. This strain represents the neotype and was isolated from meromictic (permanently stratified) Lake Polden in Norway. Cells contain BChl c and BChl a as well as chlorobactene as the major photosynthetic pigments. Acetate and propionate can be assimilated during mixotrophic growth. Chl. luteolum is incapable of assimilatory sulfate reduction, requires vitamin B 12 and salt concentrations >1% for growth.

References

1. van Gemerden, H. and Mas, J. (1995) Ecology of phototrophic sulfur bacteria. In: Anoxygenic Photosynthetic Bacteria (R. E. Blankenship, M. T. Madigan, and C. E. Bauer, eds.), pp. 49-85. Kluwer Academic Publishers, Dordrecht, The Netherlands.

2. Overmann, J. (2001) Green sulfur bacteria. In: Bergey's Manual of Systematic Bacteriology, 2 nd Edition, Volume I, (D. R. Boone and R. W. Castenholz, eds.), pp. 601-605. Springer-Verlag, New York.

3. Manske, A. K., Glaeser, J., Kuypers, M. M. M., and Overmann, J. 2005. Physiology and phylogeny of green sulfur bacteria forming a monospecific phototrophic assemblage at a depth of 100 meters in the Black Sea. Appl. Environ. Microbiol. 71: 8049-8060.

4. Frigaard, N.-U., Li, H., Gomez Maqueo Chew, A., Maresca, J. A. and Bryant, D. A. 2003. Chlorobium tepidum : insights into the physiology and biochemistry of green sulfur bacteria from the complete genome sequence. Photosynthesis Res. 78: 93-117.

5. Frigaard, N-U. and Bryant, D. A. 2004. Seeing green bacteria in a new light: genomics-enabled studies of the photosynthetic apparatus in green sulfur bacteria and filamentous anoxygenic phototrophic bacteria. Arch. Microbiol. 182: 265-276.

6. Imhoff, J. F. 2003. Phylogenetic taxonomy of the family Chlorobiaceae on the basis of 16S rRNA and fmo (Fenna-Matthews-Olson protein) gene sequences. Int. J. Syst. Evol. Microbiol. 53: 941-951.

7. Schmidle, W. 1901. Neue Algen aus dem Gebiete des Oberrheins. Beih. Bot. Zentralbl. 10: 179-180